Method for determining the voltage sensitivity of the distance between the mirrors of a fabry-perot interferometer

ABSTRACT

This publication discloses a method for determining the voltage sensitivity of the distance between the mirrors of a Fabry-Perot interferometer in a measuring device, which is intended to measure a predefined gas (e.g., CO2), of which at least one absorption maximum (ABS) or minimum is known. According to the method, at least two calibration point are defined device specifically using a reference gas (N2) in controlled conditions, in such a way that at least one of the calibration points (ABS) includes information on the control-voltage-signal-pair for one absorption maximum (ABS) of the gas being measured, and the other a corresponding pair for the reference measurement (REF), and the signal-control-voltage sensitivity is determined for the predefined gas (e.g., CO2). According to the invention, a “virtual” signal-control-voltage sensitivity curve, for example, a straight line, is formed with the aid of the calibration points formed using the reference gas (e.g., N2), ratios of the measurement points of the predefined gas (e.g., CO2) and of the corresponding values of the reference-gas curve are formed, and at least one voltage value corresponding to the minimum or maximum is defined from the ratios, in which case, on the basis of the wavelengths of the absorption minima or maxima of the gases (CO2, N2) being measured, the voltage sensitivity of the distance between the mirrors can be defined unequivocally and the necessary corrections can be made to the prevailing FPI voltage values (Vabs, Vref).

The present invention relates to a method, according to the preamble of claim 1, for determining the voltage sensitivity of the distance between the mirrors of a Fabry-Perot interferometer.

The invention also relates to a computer-software product for implementing the method.

Electrically adjustable Fabry-Perot interferometers (FPI) are commonly used as adjustable band-pass filters in, among other things, optical content measurements. The use of this method achieves considerable improvements in performance and especially in long-term stability. The use of the method according to the invention permits the control-voltage sensitivity of the distance between the mirrors of an FPI band-pass filter to be determined precisely, thus further improving the measurement accuracy of FPI technology.

For example, the long-term stability of the measurement of carbon dioxide (CO2) is based on measuring two wavelength bands in a single channel, an absorption band (ABS 4.26 μm) and a reference band (REF 3.9 μm). These two bands are typically selected using an adjustable micro-mechanical optical FPI band-pass filter, the pass band of which can be selected using voltage. The FPI control voltages corresponding to these bands are marked Vabs and Vref. The content, or a quantity proportional to it is calculated on the basis of the ratio (Tx/Rx) of the signals received from these two bands, i.e. the Tx signal value is measured using the Vabs voltage and the Rx correspondingly using the Vref voltage.

For example, the first equivalent condition for the stability of a carbon-dioxide transmitter is for the voltage control corresponding to the FPI voltages stored in the memory during factory tuning, i.e. the absorption and reference voltages and the pass bands corresponding to them, to remain unchanged over the short and long terms. For example, instability in the control voltage and rapid changes in temperature may lead to shift in the FPI pass bands and thus cause changes to appear.

The invention is intended to improve the performance of the technology described above and for this purpose to create an entirely new type of method for determining the voltage sensitivity of the distance between the mirrors of a Fabry-Perot interferometer.

The invention is based on recording, in connection with the manufacture of the FPI element, at least two measurement points for the signal-control-voltage sensitivity of a reference gas and defining, with the aid of these points, a ‘virtual’ reference-gas curve, for example, a straight line. A gas, which essentially does not absorb light in the same selected wavelength band as the gas to be measured, is used as the reference gas. In CO2 measurements, such a reference gas is, for example, N2. If there is a sufficient content of the gas being measured, the signal values of the selected absorption minima and/or maxima in the environment are measured, ratios are formed of these signal values and the corresponding signal values of the reference-gas curve, on the basis of which the natural constants, i.e. control-voltage equivalences of the absorption minima and/or maxima, are defined. This method can be applied particularly in the case of a measurement gas that is typically present in the measurement conditions. For example, the method can be reasonably used in CO2 gas measurements, as CO2 gas is one of the main background gases in the environment.

More specifically, the method according to the invention is characterized by what is stated in the characterizing portion of claim 1.

Considerable advantages are gained with the aid of the invention.

With the aid of the invention, possible wavelength-band drift in the FPI can be detected and eliminated, both effectively and reliably.

The calibration method is reliable, because it is based on the use of natural constants, the real absorption maxima or minima of real gases, so that drift will not occur in the reference values. The control voltage of the electronics and the imperfections of the system's other components are thus eliminated with the aid of unvarying natural constants.

The method in question can be used both in actual gas measurement and during calibration. The manufacture of FPI components can be simplified, as the imperfections of the manufacturing process can be compensated by the calibration procedure. In the following, the invention is examined with the aid of examples and with reference to the accompanying drawings.

FIG. 1 shows a graphical representation of the data on the FPI's control voltage, used in the method according to the invention, as a function of the signal passing through the FPI.

FIG. 2 shows the data of the figure as values in proportion to each other.

FIG. 3 shows a graphical representation of an example of one absorption-maximum search algorithm according to the invention.

A Fabry-Perot interferometer is an optical component, which includes two approximately parallel semi-reflecting mirrors in the path of the signal, the distance between which is adjusted by altering the voltage between the electrodes in the mirrors. The change in the distance between the mirrors changes the pass band of the filter. In this application, the term control voltage is used to refer to precisely the voltage intended to adjust the distance between the mirrors.

This FPI technology is disclosed in, among others, U.S. Pat. Nos. 5,561,523 and 5,646,729.

The basic equation of the Fabry-Perot interferometer is 2d=nλ  1 in which d in the distance between the mirrors of the resonator, n is an integer (=order) and λ is the wavelength. The value of the refractive index of the substance between the mirrors is assumed to be unity. In so-called long interferometers, n is usually 100-100 000. The present invention is advantageous in connection with precisely short interferometers, in which n is 1-3. The width of the pass bands of the interferometer B (=FWHM) depends of the reflection coefficient r of the mirrors and on the value of d: $\begin{matrix} {B = \frac{1 - {r\quad\lambda^{2}}}{\sqrt{r}2\pi\quad d}} & 2 \end{matrix}$

The free spectral range FSR between the different orders refers to the distance between the adjacent pass bands. The FSR can be calculated from equation (2) for the values of n n and n+1: $\begin{matrix} {{\lambda_{n} - \lambda_{n + 1}} = {{\frac{2d}{n} - \frac{2d}{n + 1}} = \frac{2d}{n\left( {n + 1} \right)}}} & (3) \end{matrix}$

It can be seen from equation (3) that the FSR increases as n diminishes. A large FSR will facilitate the removal of adjacent orders, for example, using a band-pass filter. The value d of an interferometer made using surface micro-mechanics can be 2.1 μm and n=1. The FSR then receives the value 2.1 μm.

The following describes the basic solution according to the invention, according to FIGS. 1 and 2.

To ensure that there will always be a reference curve (e.g., an N2 reference curve) available for analysis, without actually using that gas, a ‘virtual’ N2 reference curve is formed, i.e. at its simplest, a signal-FPI straight line. This straight line is formed through the calibration values T0 (at Vabs) and R0 (at Vref) of the reference gas (e.g., N2) obtained from the factory calibration and recorded in the memory of the device, according to FIG. 1. Instead of a straight line, it is also possible to use a reference curve formed from several points, which is defined and can be stored in the memory of the devices during the factory calibration. Thus, in factory calibration, the value of the control voltage for the maximum absorption (Vabs) of the gas (in this case, CO2) being measured and correspondingly for the reference voltage (Vref), as well as for the signal values corresponding to them in the reference gas, are determined with the aid of a reference gas (in this base, N2). If necessary, values corresponding to these control-voltage values can also be calculated as the distance between the mirrors. If N2 gas is used, it can be shown that the transmission curve obtained with the aid of the virtual curve corresponds well to the transmission curve close to the Vabs voltage determined with the aid of real N2 gas, according to FIG. 2.

Once a virtual reference curve has been formed, the gas to be measured (e.g., CO2) is measured in the environment of the absorption band (ABS) from the end of the previously agreed control-voltage step and the ratios of the signal values of the gas being measured and of the virtual curve. On the basis of these ratios, a new minimum (FIG. 3) is found, the position of which gives a corrected value (Vabs) for the control voltage corresponding to the absorption maximum of the carbon dioxide. Vref is formed from this value by calculation in a manner to be described later.

In practice, the FPI voltage values (Vabs and Vref) are the newest FPI voltage values. This means that, after the FPI voltage-scale correction according to the method disclosed here, the ‘N2 virtual straight line’ is also scaled according to the new Vabs and Vref, so that the T0 and R0 values being used will correspond to these new voltage values. The signal values T0 and R0 are always the newest N2 calibration values available.

Various Self-Analysis Procedures

An FPI self-analysis can always be made, according to the performance objectives and available equipment, by applying, for example, some of the following procedures:

-   -   1. A continuous automatic alternating cycle of measurements and         analysis, with a specific rhythm (e.g., 10/1) i.e.,         automatically after a cycle of, for example, 10 measurements,         one measurement including analysis is made, after which normal         measurements are continued. The analysis is continued according         to the cycle. The analysis can also be completed at one time, if         a rapid response time is not demanded.     -   2. A specific analysis interval is defined (e.g., hour, day,         week, or month), after which analysis is started automatically.         The analysis is completed at one time.     -   3. When condition limits are exceeded (pressure, temperature,         RH, etc.).     -   4. At the user's initiative.     -   5. Utilizing any of the procedures (1-4) described above, in         such a way that the user receives an error report and possible         an instruction to correct the control-voltage.     -   6. Utilizing the procedures (1-4) described above, in such a way         that the control-voltage is corrected automatically.

Irrespective of the procedure, the output results during a measurement forming part of the analysis are typically locked to the last measurement value received.

A. Self-Analysis Conditions

In addition, the following conditions, for example, are also required, in order to define a suitable time for analysis and to ensure the reliability of the analysis result. The following conditions can be applied as required:

-   -   Because the analysis described requires the gas being measured         to be present, a condition is needed for the sufficient content         of the gas. This can be presented as an absorption condition,         for example Tx/T0<0.95. The value is sensor-type specific.     -   The analysis cannot be carried out during a pronounced state of         change (the content of the gas changes rapidly or the sensor         signal is excessively noisy), i.e. the signals being measured         must be sufficiently stable: Correction based on the analysis is         made only once the stability conditions have been met. Such         conditions can be, for example, the following:         -   Content condition: Tx/Rx (or Tx/T0) must be within specific             limits before and after the analysis.         -   Noise condition: For example, continuous noise measurement             alongside the normal measurement, (e.g., 1 min) before and             after the analysis. Noise-level must be sufficiently low.     -   The lower limit to Vabs change in the FPI must be defined (to         be, for example, the same as the absorption-voltage step of the         analysis), to prevent an increase in output noise, due to         continuous very small changes in Vabs.     -   In addition, an upper limit to the cumulative Vabs correction         will be required, which will permit the original Vabs         characterization estimate to be made in its entirety.     -   One analysis can include several analysis cycles, which will         ensure that the selected new Vabs really is the new absorption         maximum. In addition, an average can be calculated from the new         Vabs values obtained. If an average is used, a condition must be         set for the divergence of the Vabs found, to ensure reliability.         B. Determining of the FPI Absorption Maximum Voltage (Vabs) of         the Measured Gas, According to FIG. 3     -   A sensor-type-specific voltage step (e.g., 0.2 V) is selected         for the self-analysis.     -   In practice, in addition to the Vabs being used, the voltage         point (e.g., Vabs−0.2 V, the left-hand side point in the figure)         that is at a distance of one voltage step is selected. The         signal value of this point is divided by the value of the         corresponding voltage of the N2 virtual straight line. If the         ratio obtained is greater than the corresponding ratio         calculated in Vabs, the analysis is then continued by         calculating a new ratio using the Vabs+0.2 V control voltage         (the third point from the left in the figure). If this ratio is         also greater than the corresponding ratio calculated in Vabs,         the analysis is terminated and the Vabs voltage is not         corrected. If the ratio with the control voltage Vabs+0.2 V is         smaller than the corresponding ratio calculated in Vabs, as in         FIG. 3, the analysis is then continued further to the right in         the figure, i.e. the signal value with the control voltage         Vabs+0.4 V is measured and the ratio of this and the straight         line's corresponding value is calculated as above. The analysis         is continued in this way, until a new Vabs is found, i.e. a new         FPI control voltage corresponding to the maximum absorption. The         sequence of measuring the measurement points in the analysis         described above can be changed.         C. Definition of a New FPI Reference Voltage     -   A new Vref corresponding to the new Vabs is now calculated. The         connection between the FPI control voltage and its void interval         are derived starting from the equilibrium condition between the         electrostatic force and the spring force of the upper mirror.         The new Vabs and Vref (or the magnitudes of the corrections made         to them) are recorded in the memory and utilized in measurement.

The method according to the invention is typically implemented with the aid of a computer program, in the processor in the equipment. 

1. A method for determining the voltage sensitivity of the distance between the mirrors in a Fabry-Perot interferometer, which is intended to measure a predefined gas (CO2), of which at least one absorption maximum (ABS) or minimum is known, in which method at least two calibration points are defined device specifically using a reference gas (N2) in controlled conditions, in such a way that at least one of the calibration points (ABS) includes information on the control-voltage signal pair for one absorption maximum (ABS) of the gas being measured, and the other a corresponding pair for the reference measurement (REF), and a corresponding signal-control-voltage definition is made for the gas being measured (CO2), characterized in that a ‘virtual’ signal-control voltage sensitivity curve, for example, a straight line, is formed with the aid of the calibration points formed using the reference gas (N2), the signal value(s) are measured in the vicinity of the preselected absorption maximum (ABS) and/or minimum, in the presence of the gas (CO2) being measured, ratio(s) are formed of the signal values of the gas (CO2) being measured and of the reference gas (N2), and the control voltage value corresponding to at least one minimum or maximum is defined from the ratio(s), in which case, on the basis of the wavelengths of the absorption minima or maxima of the gas (CO2) being measured, the voltage sensitivity of the distance between the mirrors can be defined unequivocally and the necessary corrections can be made to the prevailing FPI voltage values (Vabs, Vref).
 2. A method according to claim 1, characterized in that the gas being measured is carbon dioxide CO₂.
 3. A method according to claim 1, or to a combination of them, characterized in that the reference gas is nitrogen N₂.
 4. A method according to claim 1, or to a combination of them, characterized in that the definition is carried out automatically, in connection with the starting of the device.
 5. A method according to claim 1, or to a combination of them, characterized in that the definition is carried out at regular intervals in time.
 6. A method according to claim 1, or to a combination of them, characterized in that the definition is carried out after a specific number of measurements.
 7. A method according to claim 1, or to a combination of them, characterized in that the definition is carried out when a specific content condition of the measurement gas (CO2) is met.
 8. A method according to claim 1, or to a combination of them, characterized in that the definition is carried out on the basis of a change in an external control factor (e.g., a change in environmental conditions).
 9. A method according to claim 1, or to a combinations of them, characterized in that the definition is carried out whenever the user so wishes.
 10. A method according to claim 1, or to a combination of them, characterized in that a limit conditions is set for the content of the measurement gas (CO2).
 11. A method according to claim 1, or to a combination of them, characterized in that a lower and/or upper limit is set for the magnitude of change in the variables Vabs and Vref.
 12. A method according to claim 1, or to a combination of them, characterized in that a multipoint reference curve is formed from the reference gas (N2).
 13. A method according to claim 1, or to a combination of them, characterized in that the method is used in connection with a short Fabry-Perot interferometer.
 14. A method according to claim 1, or to a combination of them, characterized in that a device-specific definition of at least two calibration points is carried out according to the characterizing portion of claim
 1. 15. A method according to claim 1, or to a combination of them, characterized in that a new Vref value, corresponding to the new Vabs value, is calculated by deriving the connection between the FPI control voltage and the void interval from the equilibrium condition between the electrostatic force and the spring force of the upper mirror.
 16. A method according to claim 1, or to a combination of them, characterized in that the user is always given an error message in a situation requiring correction and possible an instruction to make a control-voltage correction.
 17. A method according to claim 1, or to a combination of them, characterized in that the control-voltage correction is made automatically.
 18. A computer software product for implementing according to claim
 1. 